5-(Ethylsulfanyl)thiophene-2-carboxylic acid is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic ring containing sulfur. The presence of the ethylsulfanyl group indicates that there is an ethyl group attached to a sulfur atom, which is further connected to the thiophene ring. The carboxylic acid functional group (-COOH) at the 2-position of the thiophene ring contributes to its acidic properties and enhances its reactivity, making it useful in various chemical reactions, including esterification and amidation. This compound is likely to exhibit moderate solubility in polar solvents due to the carboxylic acid group, while the thiophene ring may provide some degree of hydrophobic character. Additionally, the presence of sulfur in the structure can influence its electronic properties, potentially making it a candidate for applications in organic electronics or as a building block in the synthesis of more complex molecules. Overall, its unique structure and functional groups make it a compound of interest in organic synthesis and materials science.

5-(ethylsulfanyl)thiophene-2-carboxylic acid

101861-40-9: 5-(Ethylsulfanyl)thiophene-2-carboxylic acid is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic ring containing sulfur. The presence of the ethylsulfanyl group indicates that there is an ethyl group attached to a sulfur atom, which is further connected to the thiophene ring. The carboxylic acid functional group (-COOH) at the 2-position of the thiophene ring contributes to its acidic properties and enhances its reactivity, making it useful in various chemical reactions, including esterification and amidation. This compound is likely to exhibit moderate solubility in polar solvents due to the carboxylic acid group, while the thiophene ring may provide some degree of hydrophobic character. Additionally, the presence of sulfur in the structure can influence its electronic properties, potentially making it a candidate for applications in organic electronics or as a building block in the synthesis of more complex molecules. Overall, its unique structure and functional groups make it a compound of interest in organic synthesis and materials science.

CAS 101861-40-9

5-(ethylsulfanyl)thiophene-2-carboxylic acid

5-(Ethylthio)thiophene-2-carboxylic acid

Ref: IN-DA0005SQ

5-(Ethylsulfanyl)thiophene-2-carboxylic acid

Ref: 3D-BEA86140